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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217326Generated: October 29, 2026

Stannous Chloride → Methyl 3-amino-5-(5-methylpyridin-2-yl)benzoate

https://huagongshe.com/reaction/217326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
Reactant3-(5-Methyl-pyridin-2-yl)-5-nitro-benzoic acid methyl esterHCID 57851658—
SolventMethanolHCID 887—
ProductMethyl 3-amino-5-(5-methylpyridin-2-yl)benzoateHCID 57851018100%

Reaction Steps

To a solution of 3-(5-Methyl-pyridin-2-yl)-5-nitro-benzoic acid methyl ester (410 mg, 36.9 mmol) in methanol was added SnCl2 (1.36 g, 6.03 mmol) at room temperature. The reaction mixture was refluxed for 3 hours and then cooled. Solvent was removed in vacuo and the residue was dissolved in H2O and basified by Na2CO3 to pH=9. The mixture was extracted with CH2Cl2, and the organic phase was washed with water, brine, and dried over Na2SO4. The solvent was removed under vacuum to give 3-amino-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester (362 m g, 100%) as yellow oil. MS (M+H)=244.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193368B2
Source datasetuspto-grants-2012_06
ORD IDord-e983d14b6f7d420ab2e06258e3095b9d
Source noteuspto-grants-2012_06